Fouad Yasser, Pan Ziyan, Nafady Shaymaa, Mostafa Alaa M, Bakr Asmaa, Hagag Mahmoud, Gomaa Ahmed, Zaky Samy, Eslam Mohammed
Department of Gastroenterology, Hepatology and Endemic Medicine, Faculty of Medicine, Minia University, Main Road, Cairo, Minia, 11432, Egypt.
Storr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital and University of Sydney, Sydney, NSW, Australia.
Sci Rep. 2025 Aug 24;15(1):31098. doi: 10.1038/s41598-025-15425-7.
While metabolic dysfunction-associated fatty liver disease (MAFLD) includes the homeostatic model assessment for insulin resistance (HOMA-IR) as one of the criteria to define metabolic dysregulation, the newly proposed metabolic dysfunction-associated steatotic liver disease (MASLD) has removed this criterion. We investigated whether the HOMA-IR can serve as an independent predictive marker for significant fibrosis in subjects with MAFLD. This is a cross-sectional multicenter study. We enrolled a total of 364 patients diagnosed with MAFLD. We conducted a multiple logistic regression analysis to assess the relationship between HOMA-IR and advanced stages of liver fibrosis (F ≥ 2), as assessed by the FIB-4 score and liver stiffness measurement (LSM). Each unit increase in insulin resistance, as measured by HOMA-IR, was associated with a 16% higher likelihood of displaying significant fibrosis, as determined by a non-invasive scoring test, regardless of diabetes or BMI status. HOMA-IR was independently associated with significant fibrosis in non-diabetic (OR: 1.14, 95% CI: 1.07-1.21, P < 0.001) and diabetic (OR: 1.03, 95% CI: 1.00-1.06, P = 0.03) patients. Moreover, significant fibrosis in lean was independently linked to HOMA-IR (OR: 1.06, 95% CI: 1.01-1.12, P = 0.03) and non-lean (OR: 1.04, 95% CI: 1.02-1.07, P < 0.001) patients. Insulin resistance measured by HOMA-IR should be assessed in patients with MAFLD as a key factor of disease progression and incorporated into the disease diagnostic criteria.
虽然代谢功能障碍相关脂肪性肝病(MAFLD)将胰岛素抵抗的稳态模型评估(HOMA-IR)作为定义代谢失调的标准之一,但新提出的代谢功能障碍相关脂肪性肝病(MASLD)已删除该标准。我们研究了HOMA-IR是否可作为MAFLD患者显著纤维化的独立预测指标。这是一项横断面多中心研究。我们共纳入了364例诊断为MAFLD的患者。我们进行了多元逻辑回归分析,以评估HOMA-IR与肝纤维化晚期(F≥2)之间的关系,肝纤维化晚期通过FIB-4评分和肝脏硬度测量(LSM)进行评估。无论糖尿病或BMI状态如何,通过HOMA-IR测量的胰岛素抵抗每增加一个单位,与通过非侵入性评分测试确定的显示显著纤维化的可能性高16%相关。HOMA-IR与非糖尿病患者(OR:1.14,95%CI:1.07-1.21,P<0.001)和糖尿病患者(OR:1.03,95%CI:1.00-1.06,P=0.03)的显著纤维化独立相关。此外,瘦患者(OR:1.06,95%CI:1.01-1.12,P=0.03)和非瘦患者(OR:1.04,95%CI:1.02-1.07,P<0.001)的显著纤维化与HOMA-IR独立相关。对于MAFLD患者,应评估通过HOMA-IR测量的胰岛素抵抗,将其作为疾病进展的关键因素,并纳入疾病诊断标准。